ライフサイエンスコーパス: gene complex

1 ment in UL122-123 (the major immediate-early gene complex).

2 species (i.e., the breaking up of coadapted gene complexes).

3 l receptors that comprise the natural killer gene complex.

4 C-type lectin to map near the natural killer gene complex.

5 regulatory apparatus, exemplified by the Hox gene complex.

6 chromosome as the mouse natural killer cell gene complex.

7 t these traits are influenced by a coadapted gene complex.

8 ranscription factors encoded by the Iroquois gene complex.

9 22, to examine the overall structure of this gene complex.

10 e ends of the protein in the TFIIIA.5 S rRNA gene complex.

11 protein (MBP) gene is part of the golli-mbp gene complex.

12 a single copy into the endogenous mouse CD8 gene complex.

13 ibility complex is an invertebrate IgSF-like gene complex.

14 NF/Fas or MHC class I) are encoded in the E3 gene complex.

15 cts enhancers to specific promoters within a gene complex.

16 analyses have confirmed a role for the IL-1 gene complex.

17 n regulatory regions in the well-studied HBB gene complex.

18 lts suggest that the S locus is a huge multi-gene complex.

19 se) a neural precursor gene that reside in a gene complex.

20 pairs that define the two halves of the KIR gene complex.

21 series of duplication events resulted in the gene complex.

22 1, JC lambda 2, JC lambda 3, and JC lambda 7 gene complexes.

23 n and facilitating the formation of adaptive gene complexes.

24 ulate enhancer-promoter specificity at other gene complexes.

25 tential to be broadened to other polymorphic gene complexes.

26 at increase the stability of TFIIIA-5 S rRNA gene complexes.

27 sing organizational restraints on eukaryotic gene complexes.

28 12, between p13.2 and p12.3, close to the NK gene complex (12p13.1 to p13.2) which contains genes for

29 concept is exemplified by the mammalian Hox gene complex, a group of 39 genes which are located on 4

30 P1B and Clr-b are encoded within the NK cell gene complex, a locus that has been linked to strain-dep

31 dules are the likely precursors of coadapted gene complexes, a unit of natural selection.

32 Transcriptional enhancers in large gene complexes activate promoters over huge distances, y

33 aureus (MRSA) carrying the enterococcal vanA gene complex and expressing high level resistance to van

34 indicate that certain haplotypes in the IL-1 gene complex and in IL18 and IL4 predict an altered like

35 pecific haplotypes in the interleukin (IL)-1 gene complex and in the IL18 gene.

36 . albicans-specific assay targeting the rRNA gene complex and studied the kinetics of DNA released fr

37 ce in the transcription factor IIIA.5 S rRNA gene complex and that the rapid movements of these side

38 ch is linked to polymorphisms within the TNF gene complex and the surrounding MHC.

39 ic regions (inversions) constitute coadapted gene complexes and discuss the implications of our findi

40 teins encoded by the homeotic selector (Hox) gene complexes and increase their DNA-binding affinity a

41 E1 enhancer from the Drosophila Antennapedia gene complex (ANT-C) and the IAB5 enhancer from the Bith

42 but not all, loci within the allorecognition gene complex (ARC).

43 fy 50%-60% of noncoding positions in the HBB gene complex as regulatory or nonregulatory, with RP per

44 ion of members of the abdominal b (Abdb) Hox gene complex, as well as genes encoding bone morphogenet

45 s mutation enhanced expression of the mtrCDE gene complex but decreased expression of the mtrR gene,

46 tors, NKp80 is encoded in the natural killer gene complex, but unlike most of these, adjacent to its

47 ates the spatial expression of the AbdB HoxD gene complex by binding to regulatory elements required

48 H3 is now known to be a gene complex comprised of a minimum of two functionally

49 We report evidence that gene complexes, consisting of polycations and plasmid DN

50 rs were examined in the context of synthetic gene complexes containing modular promoters and divergen

51 ., number and size of flowers), suggesting a gene complex controlling both genetic and morphological

52 Two highly polymorphic gene complexes, detected through scent, have been implic

53 transcription unit of the Enhancer of split gene complex [E(spl)-C] exhibit an unusually high degree

54 Su(H) target genes in the Enhancer of split gene complex [E(spl)-C]; however, de novo motif analysis

55 Natural killer gene complex-encoded immunomodulatory C-type lectin-like

56 Here, we show that the spalt (sal) gene complex encodes two transcription factors that are

57 The killer immunoglobulin receptor (KIR) gene complex exhibits significant CNV.

58 gene for Panton-Valentine leukocidin and the gene complex for staphylococcal-cassette-chromosome mec

59 Distorter (SD) is an autosomal meiotic drive gene complex found worldwide in natural populations of D

60 Large gene complexes frequently use "specialized" DNA elements

61 sing NOD mice congenic for the protective NK gene complex from C57BL/6 mice.

62 nscribed spacer 1 (ITS-1) region of the rRNA gene complex from characterized Mycobacterium species.

63 mpared with C57BL/6 mice congenic for the H2 gene complex from NOD mice (B6.g7), NOD.NK1.1 mice fail

64 ontribute to gene regulation in the homeotic gene complexes from fly to mouse.

65 organs (SOs) in the absence of achaete-scute gene complex function.

66 The results show that the Manx-bobcat gene complex has a role in the development of chordate f

67 ibility complex genes, most notably the IL-1 gene complex, have been identified and novel technologie

68 ) genes on 5q35 and the Harvey ras-1-related gene complex (HRC) and the radixin pseudogene (RDPX1) on

69 organization and content of a major defense gene complex in cereals, we determined the complete sequ

70 present the vestiges of an ancient coadapted gene complex in controlling mating behavior.

71 sequencing regions flanking the beta-globin gene complex in mouse (Hbbc) and human (HBBC), we have s

72 The mtr (multiple transferable resistance) gene complex in Neisseria gonorrhoeae encodes an energy-

73 The mtr (multiple transferable resistance) gene complex in Neisseria gonorrhoeae encodes an energy-

74 of complement, and a gene near the selectin gene complex in recruitment of circulating leukocytes to

75 llels with groups of physically linked multi-gene complexes in animals and with clustered pathways fo

76 a subpopulation of Mod5 associates with tRNA gene complexes in the nucleolus.

77 The Scr-ftz region of the Antennapedia gene complex includes two known enhancers, AE1 and T1.

78 The SN-bik gene complex induced significant apoptosis in four breas

79 Expression of the mec-3/unc-86 selector gene complex induces the differentiation of the touch re

80 , common susceptibility gene or members of a gene complex involved in central nervous system immunopa

81 ic analyses show that the SD is a multilocus gene complex involving two key loci--the driver, Segrega

82 ed over time in the maintenance of 'adaptive gene complexes' involving agronomically important quanti

83 The G72/G30 gene complex is a candidate gene for schizophrenia and b

84 Interestingly, the MHC gene complex is associated with most, if not all, of the

85 des definitive evidence that the JC lambda 7 gene complex is functional.

86 IR-dependent apoptosis, indicating that this gene complex is haploinsufficient for induction of apopt

87 (human NKR-P1A), a protein encoded in the NK gene complex, is a major phenotypic marker of both these

88 Here, we describe NK gene complex knockdown (NKC(KD)) mice that lack expressi

89 ignated "non-D") that are specified by eight gene complexes known as Rh haplotypes.

90 ons and that disruption of the coadapted ETS gene complex leads to functional incompatibilities that

91 NK gene complex-linked polymorphisms, however, did not sign

92 ait loci that did not overlap with H-2 or NK gene complex loci.

93 MCMV susceptibility in genealogically and NK gene complex-Ly49 haplotype-related C57L mice.

94 At this homeotic gene complex, many different classes of cis-regulatory e

95 ly unfavorable strain in the TFIIIA.5 S rRNA gene complex may be derived from bending of the DNA that

96 ies suggest that polymorphisms of the (IL-1) gene complex may be significant risk factors for a numbe

97 2.7 cM interval within the major recognition gene complex MRC-J, a cluster of genes involved in disea

98 which is encoded in the human Natural Killer Gene Complex (NKC) adjacent to its ligand, activation-in

99 The natural killer (NK) receptor gene complex (NKC) encodes a large number of C-type lect

100 The natural killer (NK) gene complex (NKC) encodes numerous C-type lectin-like r

101 The natural killer (NK) gene complex (NKC) encodes orphan lectin-like NK cell re

102 specific polymorphisms in the natural killer gene complex (NKC) in immunosurveillance for carcinogen-

103 jection is regulated by haplotypes of the NK gene complex (NKC) that encodes multiple NK cell recepto

104 termed Chok, and loci encoded within the NK gene complex (NKC), suggesting that Chok encodes an NK c

105 helial barrier surveillance also involves NK gene complex (NKC)-encoded C-type lectin-like molecules

106 s of backcross mice demonstrated that the NK gene complex (NKC)-linked Cmv1 locus should reside betwe

107 hromosome 6 that contains the natural killer gene complex (NKC).

108 nked to the NKR-P1 receptors in the mouse NK gene complex (NKC).

109 n of the azoospermia factor (AZF), a gene or gene complex normally located on the long arm of the Y c

110 The qPCR assay targeted the rRNA gene complex of Aspergillus fumigatus.

111 The single Hox gene complex of Strongylocentrotus purpuratus contains 1

112 swine H3N2 isolates showed that the internal gene complex of the triple-reassortant viruses was assoc

113 The 500-kb Hox gene complex of this species is being sequenced in its e

114 gnition by the RAG (recombination activating gene) complex of V(D)J recombination is one contributing

115 apart in a head-to-head orientation within a gene complex on chromosome 11p15.5.

116 differential CHO-killing capacity to the NK gene complex on chromosome 6.

117 36 SARs in the human type I interferon (IFN) gene complex on chromosome 9, band p21-22, to examine th

118 CSF7), that maps close to the natural killer gene complex on human chromosome 12p13.

119 described HGT- and high sulfur (HS)-type KAP gene complex on human chromosome 21q22.11.

120 The HLA gene complex on human chromosome 6 is one of the most po

121 animal lectin family near the natural killer gene complex on mouse chromosome 6, but its protein prod

122 evolutionary trend towards larger flagellar gene complexes, operon structures have been highly disru

123 species exhibiting Batesian mimicry, a multi-gene complex or 'supergene' controls the multiple differ

124 netic recombination and establish co-adapted gene complexes, or supergenes.

125 Introduction of pNTs in a polycation-gene complex (polyplex) enhanced the extent of gene expr

126 A-tracts observed at the SARs within the IFN gene complex represent a higher level of chromatin organ

127 The coadapted gene complex responsible for this transmission advantage

128 One flanking region of the nitr gene complex shares conserved synteny with a region of m

129 The human beta-globin gene complex spans a region of 70 kb and contains numero

130 ive in mice lacking stimulator of interferon genes complex (STING), but not other innate signaling pa

131 The localization of Chok in the NK gene complex suggested that it may encode either an acti

132 Finally, the expression of the Achaete-Scute gene complex suggests that SoxNeuro acts upstream and in

133 cis-regulatory elements present in the ac-sc gene complex that are the target of the transcriptional

134 d deletions that remove the rrs-1 cluster, a gene complex that contains approximately 110 tandem copi

135 egulatory regions in the spalt/spalt-related gene complex that direct expression in the wing disc.

136 CD69 is a member of the natural-killer-cell gene complex that is expressed after activation.

137 ype lectin-like receptors, encoded in the NK gene complex, that interact with major histocompatibilit

138 ded family are located in a newly discovered gene complex, the Bearded Complex; two others reside in

139 the phylogenetic distributions of flagellar gene complexes, the flagellar gene operons existed as sm

140 The tinman gene complex (Tin-C) controls the patterning of dorsal m

141 of luciferase or beta-galactosidase reporter genes complexed to AF-20-cholesteryl-spermine resulted i

142 The HSAL gene complex was originally identified on the basis of D

143 maize (Zea mays) Rp1 disease resistance (R) gene complex was sequenced.

144 e dysregulation of genes neighboring the Prn gene complex, was responsible for the ataxic syndrome, w

145 Within the human CD8 gene complex, we identified six DNase HS clusters, four

146 To locate elements regulating the human CD8 gene complex, we mapped nuclear matrix attachment region

147 gration site of the hCD2-LCR within the mCD8 gene complex were generated, and the influence on expres

148 engrailed exists in a gene complex with invected, which together have 4 well-c

149 ng delivery of plasmid DNA encoding the CFTR gene complexed with a cationic liposome is a potential t

150 and plasmid human recombinant IL-4 and IL-10 gene complexed with cationic liposome (GAP/DLRIE) was de

151 easibility of intracavitary injection of E1A gene complexed with DC-Chol cationic liposome (DCC-E1A)

152 An E1A gene complexed with DCC-E1A cationic liposome was inject

153 of HIF-1alpha, which is encoded by the HIF1A gene, complexed with HIF-1beta, which is encoded by the

154 propose that stalled promoters help organize gene complexes within chromosomal loop domains.

155 senting the largest repeat family and immune gene complex yet produced for an individual of a ruminan